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On-demand acid-gated fluorescence switch-on in photo-generated nanospheres
Author(s) -
Jordan P. Hooker,
Florian Feist,
Laura Delafresnaye,
Federica Cavalli,
Leonie Barner,
Christopher BarnerKowollik
Publication year - 2020
Publication title -
chemical communications
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.837
H-Index - 333
eISSN - 1364-548X
pISSN - 1359-7345
DOI - 10.1039/d0cc01557a
Subject(s) - fluorescence , naphthalene , benzaldehyde , alkyne , chemistry , photochemistry , polymer , polymer chemistry , organic chemistry , optics , catalysis , physics
Herein, we introduce a fast, additive-free, ambient temperature photochemical approach - utilising the novel Diels-Alder cycloaddition of a photo-active ortho-methylbenzaldehyde (oMBA) with a terminal alkyne - for preparing functional acid-sensitive profluorescent nano-/microspheres in one step. Not previously reported, the possibility of applying such a reaction in the context of particle synthesis provides new possibilities for particle design, where multi-step reactivity can be gated into distinct steps. First, a photochemically-gated particle formation step yields a material possessing a reactive, spring-loaded intermediate at every cross-linking point. A second, on-demand step to initiate fluorescence generation subsequently imparts the properties of the chemical transformation to the material itself. The synthesised particles are narrow-disperse with an average diameter ranging from 170-380 nm.

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